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Genetic Testing and Molecular Biomarkers|October 30, 2020
Identification of Causative Variants Contributing to Nonsyndromic Orofacial Clefts Using Whole-Exome Sequencing in a Saudi FamilyHadiah Bassam Al Mahdi, Sherif Edris, Ahmed Bahieldin, et al.Genetic Testing and Molecular Biomarkers|October 16, 2020
Overexpression of Fatty Acid 2-Hydroxylase is Associated with an Increased Sensitivity to Cisplatin by Ovarian Cancer and Better PrognosesTing Qi, Dandan Wu, Zhipei Duan, et al.Genetic Testing and Molecular Biomarkers|October 8, 2020
Prognostic Role of Circular RNAs Expression in Bladder Carcinoma: A Meta-AnalysisSiyuan Wang, Shengqiang Fu, Qiang Chen, et al.Genetic Testing and Molecular Biomarkers|July 19, 2021
Upregulation of Stress-Induced Protein Kinase CK1 Delta is associated with a Poor Prognosis for patients with Hepatocellular CarcinomaHuiting Zhang, Changhong Qiu, Haifeng Zeng, et al.Genetic Testing and Molecular Biomarkers|June 2, 2021
Whole-Exome Sequencing Reveals Novel TSPAN12 Variants in Autosomal Dominant Familial Exudative VitreoretinopathyChen Chen, Mu Yang, Lulin Huang, et al.Genetic Testing and Molecular Biomarkers|January 4, 2021
Possible Association of PER2/PER3 Variable Number Tandem Repeat Polymorphism Variants with Susceptibility and Clinical Characteristics in Pancreatic CancerHasan Dagmura, Serbulent Yiğit, Ayşe Feyda Nursal, et al.Genetic Testing and Molecular Biomarkers|May 27, 2021
Influence of Lysyl oxidase Polymorphisms in Cancer Risk: An Updated Meta-analysisRungrawee Mongkolrob, Phuntila Tharabenjasin, Aporn Bualuang, et al.Genetic Testing and Molecular Biomarkers|May 26, 2021
Association of CST3 Gene with Its Protein: Cystatin C in Health and Severe Periodontal DiseaseJeneffar Roselin Christopher, Deepa Ponnaiyan, Harinath Parthasarathy, et al.Genetic Testing and Molecular Biomarkers|October 21, 2021
Identification and Validation of TREM2 in Intracranial AneurysmsJunhao Zhang, Jie Wei, Yaqi Wang, et al.Genetic Testing and Molecular Biomarkers|October 21, 2021
High-Resolution Melting Analysis for Rapid Detection of Mutations in Patients with FGFR3-Related Skeletal DysplasiasFernanda Rolemberg G Riba, Maria E S Gomes, Natana Chaves Rabelo, et al.Pageof 193